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(+)-(2R,4R)-2-AMINO-4-HYDROXY-5,5-DIMETHYLHEXANOIC-ACID

Compound with spectra: 1 NMR

(+)-(2R,4R)-2-AMINO-4-HYDROXY-5,5-DIMETHYLHEXANOIC-ACID
SpectraBase Compound ID DGTm8vpfsHc
InChI InChI=1S/C8H17NO3/c1-8(2,3)6(10)4-5(9)7(11)12/h5-6,10H,4,9H2,1-3H3,(H,11,12)/t5-,6-/m1/s1
InChIKey IAFNGKPXBRMOIM-PHDIDXHHSA-N
Mol Weight 175.23 g/mol
Molecular Formula C8H17NO3
Exact Mass 175.120843 g/mol
Enantiomer InChIKey IAFNGKPXBRMOIM-WDSKDSINSA-N

View Spectrum of (+)-(2R,4R)-2-AMINO-4-HYDROXY-5,5-DIMETHYLHEXANOIC-ACID

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O
2-amino-4-hydroxy-5,5-dimethylhexanoic acid
(-)-(2S,4S)-2-AMINO-4-HYDROXY-5,5-DIMETHYLHEXANOIC-ACID
6-Heptynoic acid, 2-amino-4-hydroxy-
THREO-(2S,4S)-GAMMA-HYDROXYGLUTAMIC-ACID-HYDROCHLORIDE;(2S,4S)-2-HYDROXY-4-AMINO-GLUTARIC-ACID-HYDROCHLORIDE
ERYTHRO-GAMMA-HYDROXYGLUTAMIC-ACID-HYDROCHLORIDE;(2R,4S)-2-HYDROXY-4-AMINO-GLUTARIC-ACID-HYDROCHLORIDE
2,6-DIAMINO-5-HYDROXYHEXANOIC ACID, IONIZED
DL-5-Hydroxylysine hydrochloride
(2S,4R)-2-Amino-5,5,5-trideuterio-4-methyl-pentanoic acid
(2S,4S)-5,5-DICHLOROLEUCINE
[6-(13)-C]-(2-S,4-S)-5,5-DICHLOROLEUCINE
Title Journal or Book Year
Synthesis of Optically Active 4-Substituted 2-Aminobutyrolactones and Homoserines by Combined Aldol/Photocyclization Reactions of Chromium Aminocarbene Complexes Journal of the American Chemical Society 1994
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